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关于正常受试者和胃酸缺乏受试者单次口服海葱苷A后的吸收情况。

On the absorption of proscillaridin A after single oral doses to normal and achlorhydric subjects.

作者信息

Andersson K E, Bergdah B, Bertler A, Redfors A

出版信息

Acta Pharmacol Toxicol (Copenh). 1977 Jan;40(1):153-60. doi: 10.1111/j.1600-0773.1977.tb02063.x.

Abstract

Proscillaridin A was given in single oral doses (1.5-2.5 mg) to normal and achlorhydric subjects. Plasma activities of the glycoside were analysed by 86Rb-technique. The absorption pattern was similar in both groups. A marked first peak of proscillaridin activity was seen after about 30 min. After a first minimum, a second peak of activity was registered within 6-12 hrs. An estimate of the amount of active glycoside absorbed during the first 12 hrs after the administration was obtained by calculating the areas under the plasma activity curves (AUC). When corrected for differences in dose per kg body weight, the mean AUC in the achlorhydric group was about 60 per cent greater than in the normal group. The results suggest that proscillaridin is rapidly absorbed; gastric acidity seems to contribute to inter-individual differences in the bio-availability of the glycoside.

摘要

将海葱苷A以单次口服剂量(1.5 - 2.5毫克)给予正常受试者和胃酸缺乏受试者。采用⁸⁶Rb技术分析该糖苷的血浆活性。两组的吸收模式相似。给药后约30分钟出现海葱苷活性的第一个明显峰值。在第一个最低值之后,6 - 12小时内记录到第二个活性峰值。通过计算血浆活性曲线下的面积(AUC)来估算给药后前12小时内吸收的活性糖苷量。当校正每千克体重剂量的差异后,胃酸缺乏组的平均AUC比正常组大约高60%。结果表明海葱苷吸收迅速;胃酸似乎导致了该糖苷生物利用度的个体差异。

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